US2024182563A1PendingUtilityA1
Anti-cntn4 antibody and use thereof
Est. expiryApr 6, 2041(~14.7 yrs left)· nominal 20-yr term from priority
Inventors:Bu Nam JeonJoo-Yeon ChungSoo Jung MoonHyunuk KimMi Young ChaJunho ChungJunyeong JinSoohyun KimJisu Chae
C07K 16/2803A61K 45/06A61K 47/6849A61P 35/00C07K 2317/622C07K 2317/23C07K 2317/24C07K 2317/76C07K 2317/92C07K 2317/52C07K 16/2818C07K 16/2827A61K 47/6803C07K 2317/565C07K 2317/31A61K 2039/505
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Claims
Abstract
The present invention relates to an anti-CNTN4 antibody or an antigen-binding fragment thereof, a pharmaceutical composition containing the same, and a use thereof for activating T cells upregulating cell-mediated immune responses, for example, for treating cancer.
Claims
exact text as granted — not AI-modified1 . An anti-CNTN4 antibody or an antigen-binding fragment thereof comprising:
a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 70; a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 88; a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 116; a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 58; a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 89; and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 115.
2 . The anti-CNTN4 antibody or antigen-binding fragment thereof according to claim 1 ,
wherein the light chain variable region comprises the amino acid sequence of SEQ ID NO: 18; and wherein the heavy chain variable region comprises the amino acid sequence of SEQ ID NO: 2.
3 . The anti-CNTN4 antibody or antigen-binding fragment thereof according to claim 1 ,
wherein the light chain variable region comprises the amino acid sequence of SEQ ID NO: 156; and wherein the heavy chain variable region comprises the amino acid sequence of SEQ ID NO: 159.
4 - 28 . (canceled)
29 . The anti-CNTN4 antibody or antigen-binding fragment thereof of claim 1 , specifically binding to a human or mouse CNTN4 protein.
30 . The anti-CNTN4 antibody or antigen-binding fragment thereof of claim 1 , binding to a human CNTN4 protein with a dissociation constant (Kd) of 1×10 −7 M or less.
31 . The anti-CNTN4 antibody or antigen-binding fragment thereof of claim 1 , increasing an activity of T cell.
32 . The anti-CNTN4 antibody or antigen-binding fragment thereof of claim 31 , wherein the T cell is CD4+ T cell or CD8+ T cell.
33 . The anti-CNTN4 antibody or antigen-binding fragment thereof of claim 1 , wherein the antigen-binding fragment is selected from the group consisting of Fab, Fab′, Fab′-SH, Fv, a single chain antibody scFv, a (Fab′)2 fragment, a single domain antibody, a diabody (dAb), and a linear antibody.
34 . The anti-CNTN4 antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody is a chimeric antibody or a humanized antibody.
35 . The anti-CNTN4 antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody is a multi-specific antibody.
36 . The anti-CNTN4 antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody is conjugated with a drug.
37 . A nucleic acid molecule encoding the antibody or antigen-binding fragment thereof of claim 1 .
38 . A recombinant expression vector comprising the nucleic acid molecule of claim 37 .
39 . A method for preventing or treating cancer, the method comprising administering, to a subject, an effective amount of the anti-CNTN4 antibody or antigen-binding fragment thereof of claim 1 , and optionally an effective amount of an additional anticancer agent.
40 . The method of claim 39 , wherein the additional anticancer agent is an immune checkpoint inhibitor or a chemotherapeutic agent.
41 . The method of claim 40 , wherein the immune checkpoint inhibitor is one or more selected from the group consisting of an anti-CTLA-4 antibody, an anti-PD-1 antibody, and an anti-PD-L1 antibody.
42 . The method of claim 39 , wherein the anti-CNTN4 antibody or antigen-binding fragment thereof, and the additional anticancer agent are simultaneously administered to a subject as a single formulation, or are simultaneously or sequentially administered to a subject as separate formulations.
43 . The method of claim 39 , wherein the cancer is a cancer that expresses CNTN4.
44 . The method of claim 39 further comprising providing an additional anticancer therapy to the subject.
45 . The method of claim 44 , wherein the additional anticancer therapy is one or more selected from the group consisting of an immune checkpoint inhibitor, a chemotherapeutic agent, and a radiotherapy.Join the waitlist — get patent alerts
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